Common genetic variants, acting additively, are a major source of risk for autism - Test2 - elhamkhani - TriplyDB

Common genetic variants, acting additively, are a major source of risk for autism

Common genetic variants, acting additively, are a major source of risk for autism

http://www.wikidata.org/entity/Q30536405

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Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture Gluten- and casein-free dietary intervention for autism spectrum conditions ehavioral Genetics The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data A novel computational biostatistics approach implies impaired dephosphorylation of growth factor receptors as associated with severity of autism.The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum Disorder Genetics of Autism Spectrum Disorder: Current Status and Possible Clinical Applications Moving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disorders The developmental transcriptome of the human brain: implications for neurodevelopmental disorders A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?Advancing the understanding of autism disease mechanisms through genetics The role of sex-differential biology in risk for autism spectrum disorder Synaptic, transcriptional and chromatin genes disrupted in autism Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs A comprehensive meta-analysis of common genetic variants in autism spectrum conditions An Overview of Autism Spectrum Disorder, Heterogeneity and Treatment Options.Folic acid and autism: What do we know?Environmental Enrichment Therapy for Autism: Outcomes with Increased Access.Copy number variation at 22q11.2: from rare variants to common mechanisms of developmental neuropsychiatric disorders.The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders.Dopaminergic variants in siblings at high risk for autism: Associations with initiating joint attention.Neural signatures of autism spectrum disorders: insights into brain network dynamics DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics.Genomic diagnosis for children with intellectual disability and/or developmental delay A de novo convergence of autism genetics and molecular neuroscience.Prioritization of neurodevelopmental disease genes by discovery of new mutations.Age of onset and family history as indicators of polygenic risk for major depression.Measuring shared variants in cohorts of discordant siblings with applications to autism Bio-collections in autism research.Gene × Environment interactions in autism spectrum disorders: role of epigenetic mechanisms.Most genetic risk for autism resides with common variation.A candidate gene association study further corroborates involvement of contactin genes in autism Research review: Polygenic methods and their application to psychiatric traits.Increasing our understanding of human cognition through the study of Fragile X Syndrome.Peptide sharing between influenza A H1N1 hemagglutinin and human axon guidance proteins.Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.The evidence for association of ATP2B2 polymorphisms with autism in Chinese Han population Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.Performance comparison of bench-top next generation sequencers using microdroplet PCR-based enrichment for targeted sequencing in patients with autism spectrum disorder Synergistic interactions between Drosophila orthologues of genes spanned by de novo human CNVs support multiple-hit models of autism

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Common genetic variants, acting additively, are a major source of risk for autism

http://www.wikidata.org/entity/Q30536405

description

2012 nî lūn-bûn

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2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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Common genetic variants, acting additively, are a major source of risk for autism

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Common genetic variants, acting additively, are a major source of risk for autism

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Common genetic variants, acting additively, are a major source of risk for autism

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Common genetic variants, acting additively, are a major source of risk for autism

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Common genetic variants, acting additively, are a major source of risk for autism

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Molecular Autism

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Common genetic variants, acting additively, are a major source of risk for autism

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A Jeremy Willsey

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Bernie Devlin

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Christopher A Walsh

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Daniel Geschwind

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Daniel Moreno-De-Luca

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David H Ledbetter

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Dorothy E Grice

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James S Sutcliffe

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Jennifer K Lowe

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Matthew W State

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P2860

Rare deletions at the neurexin 3 locus in autism spectrum disorder

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation

SHANK1 Deletions in Males with Autism Spectrum Disorder

A genomic screen of autism: evidence for a multilocus etiology.

Functional impact of global rare copy number variation in autism spectrum disorders

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Strong association of de novo copy number mutations with autism

Structural variation of chromosomes in autism spectrum disorder

PLINK: a tool set for whole-genome association and population-based linkage analyses

A unified genetic theory for sporadic and inherited autism

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Stephan J. Sanders

Donna M. Martin

Christa Lese Martin

Daniel Moreno-De-Luca

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